Investigating cell-material interactions by monitoring and analysing cell migration

Cell-material interactions can on one hand be characterised by assessing the functional state and or shape of the cells at one or different discrete periods of time, on the other hand by observing cell migration and spreading behaviour. The object of this study was to investigate the migration behaviour of fluorescently labelled cells, and to evaluate the software analysing this migration. In the present study, the behaviour of fibroblasts cells on differently structured surfaces was taken as example. In the first step, the influence of seven different lipophilic dyes (DiI, DiO, DiA, DiD, DiR, PKH2 and PKH26) on cell performance was determined taking biochemical parameters as indices. In the second step, the fluorescence characteristics of these dyes were compared regarding their applicability. In the third step, migration behaviour of DiI-labelled fibroblastic cells on plane and grooved surfaces were monitored and analysed using specific software. Our data suggest that most of the dyes have optimal characteristics for studying cell - cell interactions. Cell migration behaviour regarding migration direction and cell spreading was different on plane and grooved surfaces. It could be shown that computer-based image analysis represents a practical, quick and objective tool to quantify exactly cell migration behaviou

Optimization Of Bio-inspired Hair Sensor Arrays

Crickets use a pair of hairy appendages on their abdomen called cerci, each of which contains numerous mechano-receptive filiform hairs. These sensitive hairs can respond even to the slightest air movements, down to 0.03 mm/s, generated by the approaching predators and initiating an escape mechanism in the crickets. Bio-mimicking the cricket cerci, arrays of artificial hair sensors have been successfully fabricated using advanced MEMS techniques. Despite its appreciable performance, the actual cricket filiform hairs outperform artificial hair sensors by several orders in sensitivity. Nevertheless, more careful look at the anatomy and physiology of the cricket cerci provides new directions to be explored with MEMS technologies to realize higher sensitivities on a par with crickets’. This paper aims to provide an overview of comparisons between the actual and artificial hair sensors in terms of sensitivity, structural functionalities and robustness and draws out constructive insights to optimize sensor performance

Effects of serum and serum heat-inactivation on human bone derived osteoblast progenitor cells

Generally, heat inactivated foetal calf serum (FCS) containing media are used for the cultivation of animal and human cells. The role of serum source and serum treatment on the behaviour of cells has long been neglected. The present study was performed to investigate the effects of serum heat inactivation and serum source on trabecular bone derived progenitor cells (HBC). Furthermore, it was investigated in how far these reactions differed from those seen in bone marrow derived mesenchymal progenitor cells (HBMC) cultures. We found that HBC cultures performed differently in the presence of FCS and HS with or without heat inactivation. The reactions similar to some degree those observed in HBMC cultures. The implications of the results on cell-implant surface interaction studies are discusse

Dipole source localisation using bio-mimetic flow-sensor arrays

AbstractFlow sensor arrays can be used to extract spatio-temporal flow signatures rather than average or local flow quantities. We look at the equivalent of a fish lateral-line sensor array in air and assess the ability of our artificial hairs flow-sensor arrays to detect flow velocity distributions generated by a vibrating sphere. The measured flow patterns along a virtual lateral-line, carried out over a bandwidth of 0.3 Hz, are found to be in excellent agreement with theory and are used successfully to demonstrate source-distance determination

Surface modification and characterization of thermoplastic polyurethane

http://www.sciencedirect.com/science/article/B6TWW-4VP4TNJ-1/2/26b1d7dd60ae5bcab0cfe30ac2771c0

In vitro techniques for the assessment of neurotoxicity.

Risk assessment is a process often divided into the following steps: a) hazard identification, b) dose-response assessment, c) exposure assessment, and d) risk characterization. Regulatory toxicity studies usually are aimed at providing data for the first two steps. Human case reports, environmental research, and in vitro studies may also be used to identify or to further characterize a toxic hazard. In this report the strengths and limitations of in vitro techniques are discussed in light of their usefulness to identify neurotoxic hazards, as well as for the subsequent dose-response assessment. Because of the complexity of the nervous system, multiple functions of individual cells, and our limited knowledge of biochemical processes involved in neurotoxicity, it is not known how well any in vitro system would recapitulate the in vivo system. Thus, it would be difficult to design an in vitro test battery to replace in vivo test systems. In vitro systems are well suited to the study of biological processes in a more isolated context and have been most successfully used to elucidate mechanisms of toxicity, identify target cells of neurotoxicity, and delineate the development and intricate cellular changes induced by neurotoxicants. Both biochemical and morphological end points can be used, but many of the end points used can be altered by pharmacological actions as well as toxicity. Therefore, for many of these end points it is difficult or impossible to set a criterion that allows one to differentiate between a pharmacological and a neurotoxic effect. For the process of risk assessment such a discrimination is central. Therefore, end points used to determine potential neurotoxicity of a compound have to be carefully selected and evaluated with respect to their potential to discriminate between an adverse neurotoxic effect and a pharmacologic effect. It is obvious that for in vitro neurotoxicity studies the primary end points that can be used are those affected through specific mechanisms of neurotoxicity. For example, in vitro systems may be useful for certain structurally defined compounds and mechanisms of toxicity, such as organophosphorus compounds and delayed neuropathy, for which target cells and the biochemical processes involved in the neurotoxicity are well known. For other compounds and the different types of neurotoxicity, a mechanism of toxicity needs to be identified first. Once identified, by either in vivo or in vitro methods, a system can be developed to detect and to evaluate predictive ability for the type of in vivo neurotoxicity produced. Therefore, in vitro tests have their greatest potential in providing information on basic mechanistic processes in order to refine specific experimental questions to be addressed in the whole animal

Isolation and purification of an enzyme hydrolyzing ochratoxin A from aspergillus niger

Ochratoxin A is a mycotoxin produced by several Aspergillus and some Penicillium species which may be present in food and feed products. It can be enzymatically hydrolyzed into ochratoxin α and l-β-phenylalanine, thereby decreasing its toxicity. The ochratoxin A degradation capacity of Aspergillus niger is well known and here we report the isolation and purification of a novel enzyme from A. niger that hydrolyzes this mycotoxin. A wheat germ medium supplemented with ochratoxin A was used to produce the enzyme, which was purified from culture filtrate by acetone precipitation and anion exchange chromatography. An overall purification of 2.5-fold with a recovery of 68% and a final specific activity of 36 U/mg was obtained. The enzyme is a metalloenzyme as it was inhibited at 10 mM EDTA, whereas PMSF had no effect. The ochratoxin A hydrolytic enzyme presented a V max of 0.44 μM/min and a K m of 0.5 mM when the reaction was carried out at pH 7.5 and 37°C.Fundação para a Ciência e a Tecnologia (FCT

Stamps for submicrometer soft lithography fabricated by capillary force lithography

Lithography, capillary force • Lithography, soft • Replica molding • Stamps

Determinants of potential drug–drug interaction associated dispensing in community pharmacies in the Netherlands

OBJECTIVE: There are many drug–drug interactions (D–DI) of which some may cause severe adverse patient outcomes. Dispensing interacting drug combinations should be avoided when the risks are higher than the benefits. The objective of this study was to identify determinants of dispensing undesirable interacting drug combinations by community pharmacies in the Netherlands. METHODS: A total of 256 Dutch community pharmacies were selected, based on the dispensing of 11 undesirable interacting drug combinations between January 1st, 2001 and October 31st, 2002. These pharmacies were sent a questionnaire by the Inspectorate for Health Care (IHC) concerning their process and structure characteristics. MAIN OUTCOME MEASURE: The number of times the 11 undesirable interacting drug combinations were dispensed. RESULTS: Two hundred and forty-six questionnaires (response rate 96.1%) were completed. Dispensing determinants were only found for the D–DI between macrolide antibiotics and digoxin but not for the other 10 D–DIs. Pharmacies using different medication surveillance systems differed in the dispensing of this interacting drug combination, and pharmacies, which were part of a health care centre dispensed this interacting drug combination more often. CONCLUSION: Medication surveillance in Dutch community pharmacies seems to be effective. Although for most D–DIs no determinants were found, process and structure characteristics may have consequences for the dispensing of undesirable interacting drug combinations